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CN109265965A - A kind of preparation method of biodegradable flexible conductive electrical leads - Google Patents

A kind of preparation method of biodegradable flexible conductive electrical leads Download PDF

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Publication number
CN109265965A
CN109265965A CN201810863394.1A CN201810863394A CN109265965A CN 109265965 A CN109265965 A CN 109265965A CN 201810863394 A CN201810863394 A CN 201810863394A CN 109265965 A CN109265965 A CN 109265965A
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biodegradable
biodegradable flexible
preparation
electrical leads
polyurethane resin
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张伟
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Anhui Wei Polymerization Mstar Technology Ltd
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Anhui Wei Polymerization Mstar Technology Ltd
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Priority to CN201810863394.1A priority Critical patent/CN109265965A/en
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    • C08K7/02Fibres or whiskers
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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/20Conductive material dispersed in non-conductive organic material
    • H01B1/24Conductive material dispersed in non-conductive organic material the conductive material comprising carbon-silicon compounds, carbon or silicon
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    • H01ELECTRIC ELEMENTS
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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
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    • H01B13/06Insulating conductors or cables
    • H01B13/14Insulating conductors or cables by extrusion
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    • H01B3/30Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
    • H01B3/302Polyurethanes or polythiourethanes; Polyurea or polythiourea
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Abstract

The invention discloses a kind of preparation method of biodegradable flexible conductive electrical leads, prepared biodegradable flexible conductive wire is to use biodegradable polyurethane resin for substrate, and conductive material is functive, common coextrusion processes preparation.The features such as provided by the invention kind of biodegradable flexible conductive wire preparation method has simple process, environmentally protective, and raw material sources are extensive.Extend the active time of conductor wire so that conductor wire has good electric conductivity under high-frequency irregular folding, winding and strength pulled out condition with high elongation at break.Meanwhile biodegradable flexible conductive wire prepared by the present invention has good biodegradability, it is ensured that because update caused by conductor wire waste it is biodegradable in the natural environment, harm of the electronic waste to human body and environment can be greatly reduced.

Description

A kind of preparation method of biodegradable flexible conductive electrical leads
Technical field
The present invention relates to New-style electrical wire technical field of composite materials more particularly to a kind of biodegradable flexible conductive electrical leads Preparation method.
Background technique
With the development of science and technology facilitation, miniaturization and high performance are the main trends of Current electronic product development, lead It sends a telegraph sub- successive generations of products speed to accelerate, the conductor wire of one of important accessory of electronic product, with the upgrading of electronic product And update, become waste;Meanwhile people are during using electric wire, caused by the reasons such as strength stretching, irregular folding Conductive filament fracture in electric wire, causes entire electric wire to lose application function, so that entire electric wire becomes rubbish and loses, this has pole Big causes environmental pollution.
Existing electric wire is mainly the metal wires such as copper, aluminium as conductive core in the market, and rubber, plastics lead to as clad Cross co-extrusion modling and be processed as conductor wire, elongation at break is usually no more than 15%, because high-frequency irregular folding, winding and Strength stretch etc. reasons, electric wire fracture lead to not using thing frequent occurrence.Meanwhile the coating layer material of current electric wire exists Need tens of even more than one thousand years that could degrade in natural environment.Conductor wire leads to not because updating or damaging using then direct Become electronic waste, bad influence is generated to human body and environment.
To extend the efficient active time of conductor wire, alleviates the status in electronic waste besieged city, need a kind of biodegradable Flexible wire not only solves electric wire phenomenon of rupture caused by existing conductor wire folds because of high-frequency, winds, strongly stretches, but also Also avoid the harm caused by human body and environment of discarded conducting wire.
Summary of the invention
The object of the invention is to remedy the disadvantages of known techniques, provide it is a kind of have both environmental protection and it is easy to use can The preparation method of biodegradable flexible conductive wire.
The present invention is achieved by the following technical solutions:
A kind of preparation method of biodegradable flexible conductive electrical leads, comprises the following specific steps that:
(1) mixture of the pure and mild small molecule dihydric alcohol of polyester binary is dehydrated 2-2.5 under certain vacuum degree at 120-125 DEG C Hour, so that for water content 0.05% hereinafter, being cooled to 60-65 DEG C, discharging is spare in mixture, it is soft segment part A;
(2) using diisocyanate as hardness part B, A, B is mixed according to certain molar ratio, then heated while stirring To 100-110 DEG C, biodegradable flexible polyurethane resin matrix is prepared;
(3) by mass, 0.2-10 parts of conductive functional filler, 100 parts of biodegradable polyurethane resin matrix, 0.3-1 are taken The coupling agent of part, which is mixed evenly, prepares biodegradable flexible polyurethane resinous electricity wire inner core;
It (4) is cladding insulating layer with biodegradable flexible polyurethane resin matrix, with biodegradable flexible polyurethane resin Electric lead inner core is internal layer, is sent into extruder by being coextruded up to electric lead of the present invention.
A kind of preparation method of biodegradable flexible conductive electrical leads, polyester diol described in step (1) are that molecular weight exists Polycaprolactone diols (PCL), polyethylene glycol adipate (PEA) between 1000-4000, polybutyleneadipate refer to One or both of (PBA), small molecule dihydric alcohol is 1,4 butanediols, one of hexylene glycol, ethylene glycol.
A kind of preparation method of biodegradable flexible conductive electrical leads, certain vacuum degree described in step (1) refer to- Under the vacuum condition of 0.97Mpa.
A kind of preparation method of biodegradable flexible conductive electrical leads, diisocyanate described in step (2) are that toluene two is different Cyanate (TDI), methyl diphenylene diisocyanate (MDI), isophorone diisocyanate (IPDI), two isocyanide of hexa-methylene Acid esters (HDI), dicyclohexyl methyl hydride diisocyanate (HMDI), naphthalene diisocyanate (NDI), two isocyanide of polymethylene polyphenyl One of acid esters (PM200) and paraphenylene diisocyanate (PPDI).
A kind of preparation method of biodegradable flexible conductive electrical leads, by A, B according to certain molar ratio described in step (2) It is mixed, refers to and mixed according to the molar ratio of 1:1.05.
A kind of preparation method of biodegradable flexible conductive electrical leads, conductive functional filler described in step (3) be electrically conductive graphite, One or more of graphene, carbon nanotube, quaternary ammonium salt ionic liquid, nano metal particles, nano metal fiber mixture.
A kind of preparation method of biodegradable flexible conductive electrical leads, coupling agent described in step (3) are as follows: γ-glycidol Ether oxygen propyl trimethoxy silicane (KH560), amido functional group silane (KH550) and γ-methacryloxypropyl front three One of oxysilane (KH570).
The invention has the advantages that
(1) a kind of biodegradable flexible conductive wire provided by the invention has preparation process simple, environmentally protective, and raw material come The features such as source is extensive.
(2) present invention uses biodegradable flexible polyurethane as conducting wire substrate, and there is excellent elongation at break to be Conducting wire under high-frequency irregular folding, winding and strength pulled out condition have good electric conductivity, extend the clothes of conductor wire Use as a servant the time.
(3) biodegradable soft polyurethane matrix used in conductor wire prepared by the present invention has good biodegrade Performance, it is ensured that because update caused by conductor wire waste it is biodegradable in the natural environment, electronics rubbish can be greatly reduced Harm of the rubbish to human body and environment.
Specific embodiment
Embodiment 1
It (1) is that 2000 polycaprolactone diols (PCL) and 0.2 mole of 1.4 mixture of butanediols exist by 1 mole It 120 DEG C, under the conditions of vacuum degree -0.97Mpa, is dehydrated 2 hours, so that water content is 0.05% hereinafter, being cooled to 60 in mixture DEG C, it discharges spare, is soft segment part A;
(2) with toluene di-isocyanate(TDI) (TDI) for hardness part B, A, B is heated to 100 after 1:1.05 is mixed in molar ratio and stirred It mixes uniformly, prepares biodegradable flexible polyurethane resin matrix;
(3) by mass, 1 part of electrically conductive graphite, 100 parts of biodegradable polyurethane resin matrix, 0.3 part of coupling agent are taken (KH550) it is mixed evenly and prepares biodegradable flexible polyurethane resinous electricity wire inner core;
It (4) is cladding insulating layer with biodegradable flexible polyurethane resin, with biodegradable flexible polyurethane resin conductance Line inner core is internal layer, prepares biodegradable flexible conductive electrical leads by coextrusion processes.The biodegradable flexible conductance of preparation The elongation at break of line is greater than 200%, and conductivity is greater than 4.9 × 10-2S/cm。
Embodiment 2
(1) by 0.5 mole be 1000 polyethylene glycol adipate (PEA), 0.5 mole be 1000 to gather oneself Naphthalate (PEA) and 0.2 mole of 1.4 mixture of butanediols are under the conditions of 120 DEG C, vacuum degree -0.97Mpa, dehydration 2 Hour, so that for water content 0.05% hereinafter, being cooled to 60 DEG C, discharging is spare in mixture, it is soft segment part A;
(2) with toluene di-isocyanate(TDI) (TDI) for hardness part B, A, B is heated to 100 after 1:1.05 is mixed in molar ratio and stirred It mixes uniformly, prepares biodegradable flexible polyurethane resin matrix;
(3) by mass, 1 part of electrically conductive graphite, 100 parts of biodegradable polyurethane resin matrix, 0.4 part of coupling agent are taken (KH550) it is mixed evenly and prepares biodegradable flexible polyurethane resinous electricity wire inner core;
It (4) is cladding insulating layer with biodegradable flexible polyurethane resin, with biodegradable flexible polyurethane resin conductance Line inner core is internal layer, prepares biodegradable flexible conductive electrical leads by coextrusion processes.The biodegradable flexible conductance of preparation The elongation at break of line is greater than 200%, and conductivity is greater than 4.9 × 10-2S/cm。
Embodiment 3
(1) by 0.5 mole be 1000 polycaprolactone diols (PCL), 0.5 mole be 1000 to gather in oneself Under the conditions of 120 DEG C, vacuum degree -0.97Mpa, dehydration 2 is small for ester dihydric alcohol (PCL) and 0.2 mole of 1.4 mixture of butanediols When, so that for water content 0.05% hereinafter, being cooled to 60 DEG C, discharging is spare in mixture, it is soft segment part A;
(2) with toluene di-isocyanate(TDI) (TDI) for hardness part B, A, B is heated to 100 after 1:1.05 is mixed in molar ratio and stirred It mixes uniformly, prepares biodegradable flexible polyurethane resin matrix;
(3) by mass, 1 part of electrically conductive graphite, 100 parts of biodegradable polyurethane resin matrix, 0.3 part of coupling agent are taken (KH550) it is mixed evenly and prepares biodegradable flexible polyurethane resinous electricity wire inner core;
It (4) is cladding insulating layer with biodegradable flexible polyurethane resin, with biodegradable flexible polyurethane resin conductance Line inner core is internal layer, prepares biodegradable flexible conductive electrical leads by coextrusion processes.The biodegradable flexible conductance of preparation The elongation at break of line is greater than 200%, and conductivity is greater than 4.9 × 10-2S/cm。
Embodiment 4
(1) polybutyleneadipate that 0.5 mole is 1000 is referred to that (PBA), 0.5 mole are 1000 to gather oneself Diacid butanediol refers to that (PBA) and 0.2 mole of 1.4 mixture of butanediols under the conditions of 120 DEG C, vacuum degree -0.97Mpa, are dehydrated 2 Hour, so that for water content 0.05% hereinafter, being cooled to 60 DEG C, discharging is spare in mixture, it is soft segment part A;
(2) with toluene di-isocyanate(TDI) (TDI) for hardness part B, A, B is heated to 100 after 1:1.05 is mixed in molar ratio and stirred It mixes uniformly, prepares biodegradable flexible polyurethane resin matrix;
(3) by mass, 0.2 part of electrically conductive graphite, 100 parts of biodegradable polyurethane resin matrix, 0.3 part of coupling are taken Agent (KH550), which is mixed evenly, prepares biodegradable flexible polyurethane resinous electricity wire inner core;
It (4) is cladding insulating layer with biodegradable flexible polyurethane resin, with biodegradable flexible polyurethane resin conductance Line inner core is internal layer, prepares biodegradable flexible conductive electrical leads by coextrusion processes.The biodegradable flexible conductance of preparation The elongation at break of line is greater than 200%, and conductivity is greater than 4.9 × 10-2S/cm。
Embodiment 5
(1) by 0.5 mole be 1000 polycaprolactone diols (PCL), 0.5 mole be 1000 to gather oneself two Sour butanediol refers to (PBA) and 0.2 mole of 1.4 mixture of butanediols under the conditions of 120 DEG C, vacuum degree -0.97Mpa, and dehydration 2 is small When, so that for water content 0.05% hereinafter, being cooled to 60 DEG C, discharging is spare in mixture, it is soft segment part A;
(2) with isophorone diisocyanate (IPDI) for hardness part B, A, B are heated to after 1:1.05 is mixed in molar ratio 100 stir evenly, and prepare biodegradable flexible polyurethane resin matrix;
(3) by mass, 2 parts of carbon nanotube, 100 parts of biodegradable polyurethane resin matrix, 0.4 part of coupling agent are taken (KH560) it is mixed evenly and prepares biodegradable flexible polyurethane resinous electricity wire inner core;
It (4) is cladding insulating layer with biodegradable flexible polyurethane resin, with biodegradable flexible polyurethane resin conductance Line inner core is internal layer, prepares biodegradable flexible conductive electrical leads by coextrusion processes.The biodegradable flexible conductance of preparation The elongation at break of line is greater than 200%, and conductivity is greater than 4.9 × 10-2S/cm。
Embodiment 6
(1) by 0.5 mole be 2000 polycaprolactone diols (PCL), 0.5 mole be 1000 to gather oneself two Under the conditions of 120 DEG C, vacuum degree -0.97Mpa, dehydration 2 is small for sour glycol ester (PEA) and 0.2 mole of 1.4 mixture of butanediols When, so that for water content 0.05% hereinafter, being cooled to 60 DEG C, discharging is spare in mixture, it is soft segment part A;
(2) with polymethylene polyphenyl diisocyanate (PM200) for hardness part B, after A, B 1:1.05 mixing in molar ratio It is heated to 100 to stir evenly, prepares biodegradable flexible polyurethane resin matrix;
(3) by mass, 3 parts of ionic liquid, 100 parts of biodegradable polyurethane resin matrix, 0.4 part of coupling agent are taken (KH560) it is mixed evenly and prepares biodegradable flexible polyurethane resinous electricity wire inner core;
It (4) is cladding insulating layer with biodegradable flexible polyurethane resin, with biodegradable flexible polyurethane resin conductance Line inner core is internal layer, prepares biodegradable flexible conductive electrical leads by coextrusion processes.The biodegradable flexible conductance of preparation The elongation at break of line is greater than 200%, and conductivity is greater than 4.9 × 10-2S/cm。
Embodiment 7
(1) by 0.5 mole be 2000 polycaprolactone diols (PCL), 0.5 mole be 2000 to gather oneself two Under the conditions of 120 DEG C, vacuum degree -0.97Mpa, dehydration 2 is small for sour glycol ester (PEA) and 0.2 mole of 1.4 mixture of butanediols When, so that for water content 0.05% hereinafter, being cooled to 60 DEG C, discharging is spare in mixture, it is soft segment part A;
(2) with isophorone diisocyanate (IPDI) for hardness part B, A, B are heated to after 1:1.05 is mixed in molar ratio 100 stir evenly, and prepare biodegradable flexible polyurethane resin matrix;
(3) by mass, 2 parts of nano silver particles, 100 parts of biodegradable polyurethane resin matrix, 0.4 part of coupling are taken Agent (KH550), which is mixed evenly, prepares biodegradable flexible polyurethane resinous electricity wire inner core;
It (4) is cladding insulating layer with biodegradable flexible polyurethane resin, with biodegradable flexible polyurethane resin conductance Line inner core is internal layer, prepares biodegradable flexible conductive electrical leads by coextrusion processes.The biodegradable flexible conductance of preparation The elongation at break of line is greater than 200%, and conductivity is greater than 4.9 × 10-2S/cm。
Embodiment 8
(1) by 0.5 mole be 1000 polycaprolactone diols (PCL), 0.5 mole be 2000 to gather oneself two Under the conditions of 120 DEG C, vacuum degree -0.97Mpa, dehydration 2 is small for sour glycol ester (PEA) and 0.2 mole of 1.4 mixture of butanediols When, so that for water content 0.05% hereinafter, being cooled to 60 DEG C, discharging is spare in mixture, it is soft segment part A;
(2) with isophorone diisocyanate (IPDI) for hardness part B, A, B are heated to after 1:1.05 is mixed in molar ratio 100 stir evenly, and prepare biodegradable flexible polyurethane resin matrix;
(3) by mass, 10 parts of nanometer copper fiber, 100 parts of biodegradable polyurethane resin matrix, 0.8 part of idol are taken Connection agent (KH550), which is mixed evenly, prepares biodegradable flexible polyurethane resinous electricity wire inner core;
It (4) is cladding insulating layer with biodegradable flexible polyurethane resin, with biodegradable flexible polyurethane resin conductance Line inner core is internal layer, prepares biodegradable flexible conductive electrical leads by coextrusion processes.The biodegradable flexible conductance of preparation The elongation at break of line is greater than 200%, and conductivity is greater than 4.9 × 10-2S/cm。
Embodiment 9
(1) by 0.5 mole be 1000 polycaprolactone diols (PCL), 0.5 mole be 1000 to gather oneself two Under the conditions of 120 DEG C, vacuum degree -0.97Mpa, dehydration 2 is small for sour glycol ester (PEA) and 0.2 mole of 1.4 mixture of butanediols When, so that for water content 0.05% hereinafter, being cooled to 60 DEG C, discharging is spare in mixture, it is soft segment part A;
(2) with isophorone diisocyanate (IPDI) for hardness part B, A, B are heated to after 1:1.05 is mixed in molar ratio 100 stir evenly, and prepare biodegradable flexible polyurethane resin matrix;
(3) by mass, 10 parts of nanometer copper fiber, 100 parts of biodegradable polyurethane resin matrix, 0.8 part of idol are taken Connection agent (KH550), which is mixed evenly, prepares biodegradable flexible polyurethane resinous electricity wire inner core;
It (4) is cladding insulating layer with biodegradable flexible polyurethane resin, with biodegradable flexible polyurethane resin conductance Line inner core is internal layer, prepares biodegradable flexible conductive electrical leads by coextrusion processes.The biodegradable flexible conductance of preparation The elongation at break of line is greater than 200%, and conductivity is greater than 4.9 × 10-2S/cm。
Embodiment 10
(1) by 0.5 mole be 1000 polycaprolactone diols (PCL), 0.5 mole be 2000 to gather oneself two Under the conditions of 120 DEG C, vacuum degree -0.97Mpa, dehydration 2 is small for sour glycol ester (PEA) and 0.2 mole of 1.4 mixture of butanediols When, so that for water content 0.05% hereinafter, being cooled to 60 DEG C, discharging is spare in mixture, it is soft segment part A;
(2) methyl diphenylene diisocyanate (MDI) is hardness part B, and A, B are heated to after 1:1.05 is mixed in molar ratio 100 stir evenly, and prepare biodegradable flexible polyurethane resin matrix;
(3) by mass, 10 parts of Nano aluminum fibers, 100 parts of biodegradable polyurethane resin matrix, 1 part of coupling are taken Agent (KH560), which is mixed evenly, prepares biodegradable flexible polyurethane resinous electricity wire inner core;
It (4) is cladding insulating layer with biodegradable flexible polyurethane resin, with biodegradable flexible polyurethane resin conductance Line inner core is internal layer, prepares biodegradable flexible conductive electrical leads by coextrusion processes.The biodegradable flexible conductance of preparation The elongation at break of line is greater than 200%, and conductivity is greater than 4.9 × 10-2S/cm。
Embodiment 11
(1) by 0.5 mole be 1000 polycaprolactone diols (PCL), 0.5 mole be 2000 to gather oneself two Under the conditions of 120 DEG C, vacuum degree -0.97Mpa, dehydration 2 is small for sour glycol ester (PEA) and 0.2 mole of 1.4 mixture of butanediols When, so that for water content 0.05% hereinafter, being cooled to 60 DEG C, discharging is spare in mixture, it is soft segment part A;
(2) with hexamethylene diisocyanate (HDI) for hardness part B, A, B are heated to after 1:1.05 is mixed in molar ratio 100 stir evenly, and prepare biodegradable flexible polyurethane resin matrix;
(3) by mass, 4 parts of quaternary ammonium salt ionic liquid, 100 parts of biodegradable polyurethane resin matrix, 1 part of idol are taken Connection agent (KH560), which is mixed evenly, prepares biodegradable flexible polyurethane resinous electricity wire inner core;
It (4) is cladding insulating layer with biodegradable flexible polyurethane resin, with biodegradable flexible polyurethane resin conductance Line inner core is internal layer, prepares biodegradable flexible conductive electrical leads by coextrusion processes.The biodegradable flexible conductance of preparation The elongation at break of line is greater than 200%, and conductivity is greater than 4.9 × 10-2S/cm。
Embodiment 12
(1) by 0.5 mole be 1000 polycaprolactone diols (PCL), 0.5 mole be 2000 to gather oneself two Under the conditions of 120 DEG C, vacuum degree -0.97Mpa, dehydration 2 is small for sour glycol ester (PEA) and 0.2 mole of 1.4 mixture of butanediols When, so that for water content 0.05% hereinafter, being cooled to 60 DEG C, discharging is spare in mixture, it is soft segment part A;
(2) with paraphenylene diisocyanate (PPDI) for hardness part B, A, B is heated to 100 after 1:1.05 is mixed in molar ratio and stirred It mixes uniformly, prepares biodegradable flexible polyurethane resin matrix;
(3) by mass, 6 parts of nano-aluminium particle, 100 parts of biodegradable polyurethane resin matrix, 0.8 part of coupling are taken Agent (KH550), which is mixed evenly, prepares biodegradable flexible polyurethane resinous electricity wire inner core;
It (4) is cladding insulating layer with biodegradable flexible polyurethane resin, with biodegradable flexible polyurethane resin conductance Line inner core is internal layer, prepares biodegradable flexible conductive electrical leads by coextrusion processes.The biodegradable flexible conductance of preparation The elongation at break of line is greater than 200%, and conductivity is greater than 4.9 × 10-2S/cm。

Claims (7)

1. a kind of preparation method of biodegradable flexible conductive electrical leads, which is characterized in that comprise the following specific steps that:
(1) mixture of the pure and mild small molecule dihydric alcohol of polyester binary is dehydrated 2-2.5 under certain vacuum degree at 120-125 DEG C Hour, so that for water content 0.05% hereinafter, being cooled to 60-65 DEG C, discharging is spare in mixture, it is soft segment part A;
(2) using diisocyanate as hardness part B, A, B is mixed according to certain molar ratio, then heated while stirring To 100-110 DEG C, biodegradable flexible polyurethane resin matrix is prepared;
(3) by mass, 0.2-10 parts of conductive functional filler, 100 parts of biodegradable polyurethane resin matrix, 0.3-1 are taken The coupling agent of part, which is mixed evenly, prepares biodegradable flexible polyurethane resinous electricity wire inner core;
It (4) is cladding insulating layer with biodegradable flexible polyurethane resin matrix, with biodegradable flexible polyurethane resin Electric lead inner core is internal layer, is sent into extruder by being coextruded up to electric lead of the present invention.
2. a kind of preparation method of biodegradable flexible conductive electrical leads according to claim 1, it is characterised in that: step (1) polyester diol described in is polycaprolactone diols (PCL) of the molecular weight between 1000-4000, polyadipate second two Alcohol ester (PEA), polybutyleneadipate refer to one or both of (PBA), and small molecule dihydric alcohol is 1,4 butanediols, hexylene glycol, One of ethylene glycol.
3. a kind of preparation method of biodegradable flexible conductive electrical leads according to claim 1, it is characterised in that: step (1) certain vacuum degree described in refers under the vacuum condition of -0.97Mpa.
4. a kind of preparation method of biodegradable flexible conductive electrical leads according to claim 1, it is characterised in that: step (2) diisocyanate described in is toluene di-isocyanate(TDI) (TDI), methyl diphenylene diisocyanate (MDI), isophorone two Isocyanates (IPDI), hexamethylene diisocyanate (HDI), dicyclohexyl methyl hydride diisocyanate (HMDI), two isocyanide of naphthalene One of acid esters (NDI), polymethylene polyphenyl diisocyanate (PM200) and paraphenylene diisocyanate (PPDI).
5. a kind of preparation method of biodegradable flexible conductive electrical leads according to claim 1, it is characterised in that: step (2) mixing A, B according to certain molar ratio described in, refers to and is mixed according to the molar ratio of 1:1.05.
6. a kind of preparation method of biodegradable flexible conductive electrical leads according to claim 1, it is characterised in that: step (3) conductive functional filler described in is electrically conductive graphite, graphene, carbon nanotube, quaternary ammonium salt ionic liquid, nano metal particles, receives One or more of rice metallic fiber mixture.
7. a kind of preparation method of biodegradable flexible conductive electrical leads according to claim 1, it is characterised in that: step (3) coupling agent described in are as follows: γ-glycidyl ether oxygen propyl trimethoxy silicane (KH560), amido functional group silane (KH550) and one of γ-methacryloxypropyl trimethoxy silane (KH570).
CN201810863394.1A 2018-08-01 2018-08-01 A kind of preparation method of biodegradable flexible conductive electrical leads Pending CN109265965A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4291292A4 (en) * 2021-02-15 2024-07-03 Univ Pittsburgh Commonwealth Sys Higher Education Biodegradable leads and systems including biodegradable leads

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102186927A (en) * 2008-08-20 2011-09-14 拜尔材料科学股份公司 Antistatic or conductive polyurethanes, and method for the production thereof
CN102212265A (en) * 2011-05-12 2011-10-12 中国科学院合肥物质科学研究院 Preparation method for electroconductive polyurethane complex with anion releasing function

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102186927A (en) * 2008-08-20 2011-09-14 拜尔材料科学股份公司 Antistatic or conductive polyurethanes, and method for the production thereof
CN102212265A (en) * 2011-05-12 2011-10-12 中国科学院合肥物质科学研究院 Preparation method for electroconductive polyurethane complex with anion releasing function

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4291292A4 (en) * 2021-02-15 2024-07-03 Univ Pittsburgh Commonwealth Sys Higher Education Biodegradable leads and systems including biodegradable leads

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Application publication date: 20190125